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GM-CSF Mouse Protein

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SKU
AR26006PU-L
GM-CSF mouse recombinant protein, 50 µg
Size:
50 ug 2 ug
  $510.00
2 Weeks*
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Other products for "Csf2 or NM_009969"

Specifications
Specifications
Product Data
Species Mouse
Expression Host E. coli
Expression cDNA Clone or AA Sequence
Protein Sequence
MAPTRSPITV TRPWKHVEAI KEALNLLDDM PVTLNEEVEV VSNEFSFKKL TCVQTRLKIF EQGLRGNFTK LKGALNMTAS YYQTYCPPTP ETDCETQVTT YADFIDSLKT FLTDIPFECK KPGQK
Predicted MW 14,24 kDa
Purity >95% by SDS-PAGE & Silver staining
Presentation State Purified
Buffer Presentation State: Purified
State: Lyophilized protein
Buffer System: 50 mM acetic acid without stabilizer
Endotoxin < 0.1 ng per μg of GM-CSF
Reconstitution Method Mouse GM-CSF should be reconstituted in 50mM acetic acid or water to a concentration of 0.1 mg/ml. This solution can be diluted in water or other buffer solutions.
Preparation Lyophilized protein
Protein Description Mouse recombinant GM-CSF, aa. 125
Note Protein RefSeq: NP_035954.1
mRNA RefSeq: NM_011824
Storage The lyophilized antibody can be stored at room temperature for up to two weeks, or desiccated at -20 °C for longer. Following reconstitution store in aliquots at -20 °C. Avoid repeated freezing and thawing.
Stability Shelf life: one year from despatch.
Shipping Ambient
Reference Data
RefSeq NP_034099
Locus ID 12981
UniProt ID P01587
Cytogenetics 11 32.13 cM
Synonyms CSF2, GMCSF, Sargramostim, Molgramostin
Summary Cytokine that stimulates the growth and differentiation of hematopoietic precursor cells from various lineages, including granulocytes, macrophages, eosinophils and erythrocytes.UniProtKB/Swiss-Prot Function
Protein Categories Cytokines, Growth Factors, Secreated Proteins
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Documents
Resources

file-alt Citations

Deletion of plant-specific sugar residues in plant N-glycans by repression of GDP-D-mannose 4,6-dehydratase and β-1,2-xylosyltransferase genes
Matsuo, Kagaya, Itchoda et al
J Biosci Bioeng (2014) 118 (4), 448-54 DOI: 10.1016/j.jbiosc.2014.04.005
Cited by 12
AI Summary: In this paper, OriGene’s mouse granulocyte/macrophage-colony stimulating factor (mGM-CSF, Cat# TP303274) and human monoclonal immunoglobulin G (hIgG, Cat# TP301127) were used as recombinant proteins to assess the effectiveness of deleting plant-specific sugar residues in engineered Nicotiana benthamiana plants.
Deletion of fucose residues in plant N-glycans by repression of the GDP-mannose 4,6-dehydratase gene using virus-induced gene silencing and RNA interference
Matsuo, Matsumura
Plant Biotechnol J (2011) 9 (2), 264-81 DOI: 10.1111/j.1467-7652.2010.00553.x
Cited by 24
AI Summary: In this study, OriGene’s pCR8/GW/TOPO TA Cloning Kit was used to construct RNAi vectors for repressing the GDP-mannose 4,6-dehydratase (GMD) gene, enabling the efficient deletion of immunogenic fucose residues in plant-produced glycoproteins.
Showing 1-2 of 2 papers.
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